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盐酸戊乙奎醚通过抑制内皮细胞中 p38MAPK 的激活来减轻 LPS 诱导的 iNOS 产生。

Penehyclidine hydrochloride attenuates LPS-induced iNOS production by inhibiting p38 MAPK activation in endothelial cells.

机构信息

Department of Anesthesiology, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei, People's Republic of China.

出版信息

Mol Biol Rep. 2012 Feb;39(2):1261-5. doi: 10.1007/s11033-011-0857-4. Epub 2011 May 21.

Abstract

The aim of this study was to investigate the inhibitory effect of penehyclidine hydrochloride (PHC) on lipopolysaccharide (LPS)-induced nitric oxide (NO) and inducible nitric oxide synthase (iNOS) production in human endothelial cell. Cultured endothelial cells were pretreated with PHC, followed by LPS treatment. NO activity were determined. iNOS expression and p38 mitogen-activated protein kinase (p38 MAPK) protein expression were measured by Western blot analysis. LPS treatment significantly induced p38 MAPK activation, iNOS expression, and NO production, which could be attenuated by 2 μg/ml PHC pretreatment. Furthermore, our study showed LPS-induced NO production and iNOS expression were suppressed by p38 MAPK inhibitor SB203580 pretreatment. We concluded that PHC attenuates NO production and iNOS expression by suppressing the activation of p38 MAPK pathway, thereby implicating a mechanism by which PHC may exert its protective effects against LPS-induced endothelial cell injury.

摘要

本研究旨在探讨盐酸戊乙奎醚(PHC)对脂多糖(LPS)诱导的人内皮细胞一氧化氮(NO)和诱导型一氧化氮合酶(iNOS)产生的抑制作用。培养的内皮细胞先用 PHC 预处理,然后用 LPS 处理。测定 NO 活性。通过 Western blot 分析测定 iNOS 表达和 p38 丝裂原活化蛋白激酶(p38 MAPK)蛋白表达。LPS 处理显著诱导 p38 MAPK 激活、iNOS 表达和 NO 产生,而 2μg/ml PHC 预处理可减弱其诱导作用。此外,我们的研究表明,p38 MAPK 抑制剂 SB203580 预处理可抑制 LPS 诱导的 NO 产生和 iNOS 表达。我们的结论是,PHC 通过抑制 p38 MAPK 通路的激活来减弱 NO 产生和 iNOS 表达,从而暗示 PHC 可能通过这种机制发挥其对 LPS 诱导的内皮细胞损伤的保护作用。

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